ENST00000697149.1:c.1708G>C
|
ENSP00000513138.1:n.1708G>C
|
|
ENST00000697150.1:c.1766G>C
|
ENSP00000513139.1:n.1766G>C
|
|
ENST00000697151.1:c.1699G>C
|
ENSP00000513140.1:n.1699G>C
|
|
ENST00000697164.1:c.1779G>C
|
ENSP00000513153.1:p.Arg593Ser
|
|
ENST00000697165.1:c.1566G>C
|
ENSP00000513154.1:p.Arg522Ser
|
|
ENST00000347310.10:c.1869G>C
MANE Select
|
ENSP00000321345.5:p.Arg623Ser
|
|
ENST00000637002.1:c.1260G>C
|
ENSP00000490340.1:p.Arg420Ser
|
|
ENST00000347310.9:c.1869G>C
|
ENSP00000321345.5:p.Arg623Ser
|
|
ENST00000395227.2:c.663G>C
|
ENSP00000378652.2:p.Arg221Ser
|
|
ENST00000425614.3:c.1104G>C
|
ENSP00000387640.2:p.Arg368Ser
|
|
ENST00000473881.2:c.*695G>C
|
ENSP00000486667.1:n.*695G>C
|
|
NM_144701.2:c.1869G>C
|
NP_653302.2:p.Arg623Ser
|
|
XM_005270516.2:c.1107G>C
|
XP_005270573.1:p.Arg369Ser
|
|
XM_011540789.1:c.1959G>C
|
XP_011539091.1:p.Arg653Ser
|
|
XM_011540790.1:c.1869G>C
|
XP_011539092.1:p.Arg623Ser
|
|
XM_011540791.1:c.1869G>C
|
XP_011539093.1:p.Arg623Ser
|
|
XM_011540790.3:c.1869G>C
|
XP_011539092.1:p.Arg623Ser
|
|
XM_011540791.3:c.1869G>C
|
XP_011539093.1:p.Arg623Ser
|
|
XR_001736993.1:n.1949G>C
|
|
|
NM_144701.3:c.1869G>C
MANE Select
|
NP_653302.2:p.Arg623Ser
|
|